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  5. NDC Package Code: 53808-1121-1 Ondansetron Hydrochloride

NDC Package 53808-1121-1 Ondansetron Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
53808-1121-1
Package Description:
30 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
53808-1121
Proprietary Name:
Ondansetron Hydrochloride
Usage Information:
Ondansetron tablets are indicated for the prevention of nausea and vomiting associated with:highly emetogenic cancer chemotherapy, including cisplatin greater than or equal to 50 mg/m2initial and repeat courses of moderately emetogenic cancer chemotherapyradiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomenOndansetron tablets are also indicated for the prevention of postoperative nausea and/or vomiting.
11-Digit NDC Billing Format:
53808112101
NDC to RxNorm Crosswalk:
  • RxCUI: 198052 - ondansetron HCl 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG (as ondansetron HCl dihydrate 5 MG) Oral Tablet
    • Labeler Name:
    Doh Central Pharmacy
    Sample Package:
    No
    Start Marketing Date:
    09-14-2017
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 53808-1121-1?

    The NDC Packaged Code 53808-1121-1 is assigned to a package of 30 tablet, film coated in 1 blister pack of Ondansetron Hydrochloride, labeled by Doh Central Pharmacy. The product's dosage form is and is administered via form.

    Is NDC 53808-1121 included in the NDC Directory?

    No, Ondansetron Hydrochloride with product code 53808-1121 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Doh Central Pharmacy on September 14, 2017 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 53808-1121-1?

    The 11-digit format is 53808112101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-153808-1121-15-4-253808-1121-01